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CHEMBRDG-BB 6619297, with the molecular formula C26H26N2O2, is a chemical compound identified as a kinase inhibitor. Kinase inhibitors are a class of pharmaceuticals that block the action of specific enzymes known as kinases, which play a crucial role in cell signaling and regulation. This potentially bioactive compound has therapeutic applications in treating various conditions, including cancer, inflammatory diseases, and other disorders related to abnormal cell proliferation and signaling. Further research is required to fully understand the properties and potential uses of CHEMBRDG-BB 6619297.

70132-87-5

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70132-87-5 Usage

Uses

Used in Pharmaceutical Industry:
CHEMBRDG-BB 6619297 is used as a kinase inhibitor for targeting specific enzymes involved in cell signaling and regulation. Its ability to block these enzymes makes it a promising candidate for the development of therapeutic agents to treat cancer, inflammatory diseases, and other conditions related to abnormal cell proliferation and signaling.
Used in Cancer Treatment:
CHEMBRDG-BB 6619297 is used as an anticancer agent for inhibiting the activity of kinases that are often dysregulated in cancer cells. By blocking these enzymes, it can potentially suppress tumor growth, prevent metastasis, and enhance the effectiveness of conventional cancer therapies.
Used in Inflammatory Disease Management:
CHEMBRDG-BB 6619297 is used as an anti-inflammatory agent for modulating the activity of kinases involved in inflammatory responses. Its ability to inhibit these enzymes can help reduce inflammation, alleviate pain, and improve the overall quality of life for patients suffering from inflammatory diseases.
Used in Drug Discovery and Development:
CHEMBRDG-BB 6619297 serves as a valuable compound in drug discovery and development efforts. Its kinase inhibitory properties make it a useful tool for researchers to study the role of kinases in various diseases and to develop novel therapeutic agents targeting these enzymes.
Used in Research and Development of Targeted Therapies:
CHEMBRDG-BB 6619297 is used as a research tool for the development of targeted therapies. Its ability to selectively inhibit specific kinases can help researchers identify potential therapeutic targets and design drugs that specifically target these enzymes, leading to more effective and less toxic treatments for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 70132-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,3 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70132-87:
(7*7)+(6*0)+(5*1)+(4*3)+(3*2)+(2*8)+(1*7)=95
95 % 10 = 5
So 70132-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClNO4/c1-20-11-5-2-9(3-6-11)14(17)12-8-10(16(18)19)4-7-13(12)15/h2-8H,1H3

70132-87-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4'-methoxy-5-nitro-benzophenone

1.2 Other means of identification

Product number -
Other names 2-Chlor-4'-methoxy-5-nitro-benzophenon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70132-87-5 SDS

70132-87-5Relevant academic research and scientific papers

PROCESS FOR THE PREPARATION OF 6-(PERFLUOROALKYL)URACIL COMPOUNDS FROM CARBAMATE COMPOUNDS

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Page 19, (2010/02/06)

An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having structural formula (I) from carbamate compounds having structural formula (II).

Synthesis and antitumor activity of novel benzophenone derivatives

Kumazawa, Eiji,Hirotani, Kenji,Burford, S. Clifford,Kawagoe, Keiichi,Miwa, Tamotsu,Mitsui, Ikuo,Ejima, Akio

, p. 1470 - 1474 (2007/10/03)

Novel benzophenone derivatives were synthesized and screened for cytotoxic and antitumor activity. Friedel-Crafts condensation was employed to construct the benzophenone skeleton. Among the compounds synthesized, morpholino and thiomorpholino benzophenones 3a-d exhibited potent cytotoxic activity against P388 murine leukemia and PC-6 human lung carcinoma cells in vitro, and compounds 3a, 3c, and 3j, when administered intraperitoneally, showed significant antitumor activity against the malignant ascites caused by intraperitoneal inoculation of P388 cells in mice.

(Benzoylphenyl)piperidines: A new class of immunomodulators

Bellamy,Chazan,Dodey,Dutartre,Ou,Pascal,Robin

, p. 1545 - 1552 (2007/10/02)

A series of (benzoylphenyl)piperidines has been synthesized and evaluated for activity as immunomodulators. Several of these compounds show good activity in primary screening on the basis of the lymphocytes mitogenic response to Con A, PHA, and PWM. A chloro group in position 4 of the benzoyl moiety as well as an amino group (or a carbamate derivative) para to the piperidine nucleus seems to be essential for activity. The depicted compounds may be considered as the first examples of a new series of immunomodulators.

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